(Q46509027)

English

Polymorphism of the solute carrier family 12 (sodium/chloride transporters) member 3, SLC12A3, gene at exon 23 (+78G/A: Arg913Gln) is associated with elevation of urinary albumin excretion in Japanese patients with type 2 diabetes: a 10-year longitu

scientific article published on 25 May 2005

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Polymorphism of the solute carrier family 12 (sodium/chloride transporters) member 3, SLC12A3, gene at exon 23 (+78G/A: Arg913Gln) is associated with elevation of urinary albumin excretion in Japanese patients with type 2 diabetes: a 10-year longitudinal study (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

type 2 diabetes

1 reference

based on heuristic

inferred from title

Hirotaka Watada

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

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K Nishiyama

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Y Tanaka

2

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Europe PubMed Central

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12 January 2020

K Nakajima

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

A Mokubo

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Y Atsumi

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

K Matsuoka

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

T Hirose

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

T Nomiyama

9

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

S Maeda

10

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Europe PubMed Central

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12 January 2020

R Kawamori

11

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12 January 2020

publication date

25 May 2005

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

48

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Europe PubMed Central

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12 January 2020

7

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Europe PubMed Central

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12 January 2020

1335-1338

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15915338%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Familial factors determine the development of diabetic nephropathy in patients with IDDM.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term results of the Kumamoto Study on optimal diabetes control in type 2 diabetic patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephropathy in diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The renal tubular Na-Cl co-transporter (NCCT): a potential genetic link between blood pressure and bone density?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and classification of diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial predisposition to renal disease in two generations of Pima Indians with type 2 (non-insulin-dependent) diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of micro- and macroalbuminuria, arterial hypertension, retinopathy and large vessel disease in European Type 2 (non-insulin-dependent) diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of diabetic nephropathy: evidence for major and minor gene effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/15915338

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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